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. Author manuscript; available in PMC: 2021 Apr 1.
Published in final edited form as: J Am Chem Soc. 2020 Mar 20;142(13):5974–5979. doi: 10.1021/jacs.0c01332

Table 2.

Scope of Enantioselective Amination Reactiona

graphic file with name nihms-1621090-t0006.jpg
a

Yields and enantioselectivities are for isolated material following chromatography on silica gel and are the average of two experiments. Reactions were conducted on 0.5 mmol scale.

b

Reaction was run at room temperature.

c

Reaction was run in dichloromethane.

d

Reactions were run at 0 °C with substitution of TRIP-disulfide for thiol.